FERROX 260308 Parallel Bars with Platform Instruction Manual
Read the instructions and use the product as directed according to its function.
- FIXER LE TUBE DE SOUTIEN BLANC, CYLINDRIQUE, À SON SUPPORT SUR LE SOCLE,
- INSERT THE WHITE CYLINDRICAL SUPPORT TUBE INTO THE DESIGNATED FITTING ON THE BASE
ATTENTION: POUR L’INSTALLATION CORRECTE IL EST INDISPENSABLE DE COMMENCER L’INSTALLATION A’ PARTIR DU TROU PLUS BAS (A)
NOTE: TO ENSURE CORRECT ASSEMBLY OF THE ITEM IT IS NECESSARY TO START AT THE BOTTOM HOLE AND PROCEED FROM THERE UPWARDS
ASSEMBLY OF PARALLEL BARS
- THE ASSEMBLED PARTS (B) PROVIDE FOR THE FIXATION OF THE HANDRAIL TO ITS SUPPORTING STAND. SCREW-NUT (B1) HAS TO BE TIGHTENED WITHOUT IMPEDING THE ROTATION OF THE HANDRAIL, TO ALLOW FOR ITS
ADJUSTMENT IN BREADTH.
FOR ADJUSTMENT IN BREADTH, RELEASE LEVER (C) AND GENTLY PUSH AND TURN (TO THE LEFT/RIGHT) CHROMED SUPPORT (D).
THE HEIGHT OF THE PARALLEL BARS IS CORRECTLY AND SECURELY ADJUSTED, ONCE
THE FASTENER TIGHTLY SITS IN ONE OF THE SPECIFICALLY DESIGNED NOTCHES
THE NOTCH POSITIONING FOR HEIGHT ADJUSTMENT IS: WRONG.
REFER TO FIGURE 3 FOR CORRECT
ALIGNMENT.
THE NOTCH POSITIONING FOR HEIGHT ADJUSTMENT IS: CORRECT.
IN THIS ALIGNMENT THE FASTENER (A) IS CORRECTLY POSITIONED TO SNAP IN THE DESIGNATED NOTCH.
IDENTIFICATION LABEL
WARNINGS
CLASSIFICATION AND USE
PARALLEL BARS WITH PLATFORM: 260308
Read the instructions and use the product as directed according to its function.
Do not use the product in a way other than its intended purpose.
INTENDED USE
Parallel bars with base for continuous use in manned hospital environment.
Immobilised patients with simple fractures or residents in aged-care facilities, who require a firm support, adjustable in height and width for a greater feeling of security.
TYPE OF PATIENT
Adults who need to learn how to walk again or simply to move around safely inside a room and along a path.
PLACE OF USE
Hospitals, specialised clinics, aged-care facilities
OPERATORS QUALIFIED TO USE THE PRODUCT
All healthcare professionals, physiotherapists, and related industries.
The instructions given to the patient by the healthcare professional.
CONTRAINDICATIONS
Follow the safety instructions in user manual.
Not suitable for sports use.
OTHER INDICATIONS
The device does not have essential levels of performance.
Report all serious incidents that occur due to the device. Report the incident to the manufacturer and the competent authority
At the end of its life, the product must be disposed of in accordance with local regulations and taken to specific waste collection facilities.
DATA SHEET
CARRYING CAPACITY OF THE DEVICE
DECLARATION OF CONFORMITY UE
MDR 2017/745
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